N-terminal pro-B-type natriuretic peptide and the prediction of primary cardiovascular events: results from 15-year follow-up of WOSCOPS (original) (raw)

Welsh, P. ORCID logoORCID: https://orcid.org/0000-0002-7970-3643, Doolin, O., Willeit, P., Packard, C. ORCID logoORCID: https://orcid.org/0000-0002-2386-9927, Macfarlane, P., Cobbe, S., Gudnason, V., Di Angelantonio, E., Ford, I. ORCID logoORCID: https://orcid.org/0000-0001-5927-1823 and Sattar, N. ORCID logoORCID: https://orcid.org/0000-0002-1604-2593(2013) N-terminal pro-B-type natriuretic peptide and the prediction of primary cardiovascular events: results from 15-year follow-up of WOSCOPS.European Heart Journal, 34(6), pp. 443-450. (doi: 10.1093/eurheartj/ehs239)

Abstract

Aims:To test whether N-terminal pro-B-type natriuretic peptide (NT-proBNP) was independently associated with, and improved the prediction of, cardiovascular disease (CVD) in a primary prevention cohort. Methods and results: In the West of Scotland Coronary Prevention Study (WOSCOPS), a cohort of middle-aged men with hypercholesterolaemia at a moderate risk of CVD, we related the baseline NT-proBNP (geometric mean 28 pg/mL) in 4801 men to the risk of CVD over 15 years during which 1690 experienced CVD events. Taking into account the competing risk of non-CVD death, NT-proBNP was associated with an increased risk of all CVD [HR: 1.17 (95% CI: 1.11–1.23) per standard deviation increase in log NT-proBNP] after adjustment for classical and clinical cardiovascular risk factors plus C-reactive protein. N-terminal pro-B-type natriuretic peptide was more strongly related to the risk of fatal [HR: 1.34 (95% CI: 1.19–1.52)] than non-fatal CVD [HR: 1.17 (95% CI: 1.10–1.24)] (P= 0.022). The addition of NT-proBNP to traditional risk factors improved the C-index (+0.013; P < 0.001). The continuous net reclassification index improved with the addition of NT-proBNP by 19.8% (95% CI: 13.6–25.9%) compared with 9.8% (95% CI: 4.2–15.6%) with the addition of C-reactive protein. N-terminal pro-B-type natriuretic peptide correctly reclassified 14.7% of events, whereas C-reactive protein correctly reclassified 3.4% of events. Results were similar in the 4128 men without evidence of angina, nitrate prescription, minor ECG abnormalities, or prior cerebrovascular disease. Conclusion: N-terminal pro-B-type natriuretic peptide predicts CVD events in men without clinical evidence of CHD, angina, or history of stroke, and appears related more strongly to the risk for fatal events. N-terminal pro-B-type natriuretic peptide also provides moderate risk discrimination, in excess of that provided by the measurement of C-reactive protein.

Item Type: Articles
Status: Published
Refereed: Yes
Glasgow Author(s) Enlighten ID: Cobbe, Professor Stuart and Welsh, Professor Paul and Doolin, Ms Orla and Macfarlane, Professor Peter and Sattar, Professor Naveed and Ford, Professor Ian and Packard, Professor Chris
Authors: Welsh, P., Doolin, O., Willeit, P., Packard, C., Macfarlane, P., Cobbe, S., Gudnason, V., Di Angelantonio, E., Ford, I., and Sattar, N.
College/School: College of Medical Veterinary and Life Sciences > School of Health & Wellbeing > Robertson CentreCollege of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health
Journal Name: European Heart Journal
Journal Abbr.: Eur. Heart J.
Publisher: Oxford University Press on behalf of European Society of Cardiology
ISSN: 0195-668X
ISSN (Online): 1522-9645
Published Online: 31 August 2012
Copyright Holders: Copyright © 2012 The Authors
First Published: First published in European Heart Journal 34(6):443-450
Publisher Policy: Reproduced under a Creative Commons License

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Funder and Project Information

1

NT-proBNP as a predictor of vascular events in WOSCOPS: using modern epidemiological techniques to test clinical utility of a biomarker

Paul Welsh

FS/10/005/28147

RI CARDIOVASCULAR & MEDICAL SCIENCES

Deposit and Record Details

ID Code: 69433
Depositing User: Mrs Marie Cairney
Datestamp: 10 Sep 2012 15:44
Last Modified: 01 May 2025 22:07
Date of first online publication: 31 August 2012
Date Deposited: 14 December 2015